Effect of Adsorbent Pretreatments on Methanol Content and Quality of Jujube Wine
Related Experiment Video
Updated: Apr 15, 2026

Optimization of Processing of Tiebangchui with Highland Barley Wine Based on the Box-Behnken Design Combined with the Entropy Method
Published on: May 19, 2023
Ang Li1, Jianhua Guo1, Wan Zhao1
1College of Food and Biological Engineering, Qiqihar University, Qiqihar 161006, China.
Abstract:
Jujube wine production faces the technical challenge of excessive methanol formation due to the high pectin content of the raw material. This study systematically compared five pre-fermentation treatments (pectinase, chitosan, bentonite, gelatin, and diatomite) for their effects on the methanol content and overall quality of jujube wine, aiming to identify an adsorbent pretreatment strategy that effectively reduces methanol levels while preserving wine quality. Using pectinase treatment as a reference control (representing conventional industrial pectin degradation), the results showed that all adsorbent treatments reduced the pectin content in jujube juice, thereby influencing methanol generation in the fermented wine. Notably, chitosan pretreatment exhibited the most pronounced methanol reduction (113.35 mg/L), which was 59.20% lower than that of the pectinase reference group (277.65 mg/L), and remained far below the methanol limits stipulated by Chinese, EU, and OIV standards (≤400 mg/L). This effectiveness is attributed to the positively charged nature of chitosan, which efficiently removes negatively charged pectin through electrostatic adsorption, thereby blocking methanol formation at the source. Chitosan treatment also resulted in the highest alcohol content (5.82%) and significantly reduced organic acid levels but concurrently led to a slight decrease in some key aroma esters. However, sensory evaluation revealed that jujube wine produced from the chitosan-pretreated juice maintained a harmonious overall taste profile, with an overall score comparable to that of the pectinase reference group. In comparison, bentonite and gelatin showed moderate effectiveness, while diatomite performed poorly. Notably, although pectinase treatment yielded the lowest pectin content, it paradoxically resulted in the highest methanol levels, highlighting the critical mechanism of pectin degradation (rather than removal) promoting methanol formation. In conclusion, chitosan was recommended as an effective pre-fermentation treatment strategy for producing jujube wine with a significantly reduced methanol risk. This study provided a theoretical basis and technical reference for the safe, high-quality industrial production of jujube wine.
More Related Videos
07:05Author Spotlight: Eco-Friendly Extraction of Bioactive Compounds Using Polyol-Based Microwave-Assisted Techniques
Published on: August 23, 2024
08:09A Novel Method for the Pentosan Analysis Present in Jute Biomass and Its Conversion into Sugar Monomers Using Acidic Ionic Liquid
Published on: June 1, 2018
Related Concept Videos
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat...
Preparation of Alcohols via Substitution Reactions
Alcohols can be synthesized from alkyl halides via nucleophilic substitution reactions. The highly polar carbon-halogen bond in the substrate makes halide a good leaving group. The hydroxide ion or water can act as a nucleophile to take the place of halide and form an alcohol. The substitution reactions occur via two different reaction pathways, SN1 or SN2, depending on the nature of carbon attached to the halide.
Primary alcohols are synthesized from primary alkyl halides, and the...
Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Ethers from Alkenes: Alcohol Addition and Alkoxymercuration-Demercuration
Ethers can also be prepared from alkenes through acid-catalyzed addition of alcohols and alkoxymercuration–demercuration.
Preparation of Ethers by Acid-Catalyzed Addition of Alcohol to Alkenes
The acid-catalyzed addition of alcohol to an alkene involves treating the alkene with an excess of alcohol in the presence of an acid catalyst to form an ether under suitable conditions. The hydrogen will add to the less substituted carbon so that the nucleophile can attack the more...
Acid-Catalyzed Dehydration of Alcohols to Alkenes